Thus, it is reasonable to ask how powerful—and useful—could be a large-scale association study using SNP microarrays in crosses between divergent outbred populations.

SNP-based microarrays identify unbalanced chromosomal abnormalities (loss and/or gain of DNA) in patients with unexplained abnormal phenotypes such as intellectual disability, dysmorphic features ...

SNP microarrays are capable of detecting a large number of subtle DNA alterations and/or abnormal alterations related to chromosome copy number (aneuploidy) or chromosome structural rearrangements. In ...

SNP Association in Autism Single nucleotide polymorphism microarrays have introduced the possibility of unbiased association screens, or GWAS, but can also be utilized for very-high-density ...

While microarrays provide information about the presence or absence of a genetic variant, the Diversity SNP panel produces dynamic, multi-faceted information across a broad spectrum of the population.

The SNP Array 6.0 is a single microarray that measures more than 1.8 million markers for genetic variation, according to the company. It consists of 906,600 SNPs and 946,000 copy-number probes.

Archived DNA from 18 blood samples obtained for routine clinical CLL analysis was evaluated, in parallel with the standard CLL FISH panel, at the following SNP microarray probe densities: 10K2.0 ...

Abstract 11622 Background: SNP microarray can detect Copy Number Alterations (CNAs) which could be predictive of response and can help define therapeutic strategies. Our aim is to improve conventional ...